The influence of silanes on the scorching time of rubber compounds and some properties of natural rubber vulcanizates crosslinked with diurethane

Polimery ◽  
1982 ◽  
Vol 27 (03) ◽  
pp. 93-96
Author(s):  
BOLESLAW JURKOWSKI ◽  
ALEKSANDER JEDRASZAK
Polymers ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 39
Author(s):  
Bashir Algaily ◽  
Wisut Kaewsakul ◽  
Siti Salina Sarkawi ◽  
Ekwipoo Kalkornsurapranee

The property retentions of silica-reinforced natural rubber vulcanizates with various contents of a self-healing modifier called EMZ, which is based on epoxidized natural rubber (ENR) modified with hydrolyzed maleic anhydride (HMA) as an ester crosslinking agent plus zinc acetate dihydrate (ZAD) as a transesterification catalyst, were investigated. To validate its self-healing efficiency, the molecular-scale damages were introduced to vulcanizates using a tensile stress–strain cyclic test following the Mullins effect concept. The processing characteristics, reinforcing indicators, and physicomechanical and viscoelastic properties of the compounds were evaluated to identify the influences of plausible interactions in the system. Overall results demonstrate that the property retentions are significantly enhanced with increasing EMZ content at elevated treatment temperatures, because the EMZ modifier potentially contributes to reversible linkages leading to the intermolecular reparation of rubber network. Furthermore, a thermally annealing treatment of the damaged vulcanizates at a high temperature, e.g., 120 °C, substantially enhances the property recovery degree, most likely due to an impact of the transesterification reaction of the ester crosslinks adjacent to the molecular damages. This reaction can enable bond interchanges of the ester crosslinks, resulting in the feasibly exchanged positions of the ester crosslinks between the broken rubber molecules and, thus, achievable self-reparation of the damages.


1980 ◽  
Vol 53 (2) ◽  
pp. 313-320 ◽  
Author(s):  
J. L. Thiele ◽  
R. E. Cohen

Abstract As with polybutadiene and SBR compounds, filled and unfilled vulcanizates of natural rubber exhibit long transients in their linear thermal expansion response following sudden changes in temperature. This is particularly noticeable when the materials are prestretched well beyond the point of thermoelastic inversion. Incorporation of 50 phr of carbon black significantly reduces the magnitude of the linear thermal expansion coefficient for natural rubber compounds; this reduction is greater than expected on the basis of comparisons with previous data on filled SBR vulcanizates. Changes in the surface chemistry of the filler have little effect on the thermal expansion behavior. For the unfilled vulcanizate, an equation based on rubber elasticity theory was successful in predicting the strain dependence of the linear thermal expansion coefficient up to moderate levels of strain. At higher strains the large deviations from theory were observed.


2016 ◽  
Vol 89 (3) ◽  
pp. 406-418 ◽  
Author(s):  
Nuchanart Onchoy ◽  
Pranee Phinyocheep

ABSTRACT Functionalization of NR with a bromine atom was developed and explored for its application in a silica-reinforced NR system. Two possible pathways were investigated: the direct addition of a bromine atom using N-bromosuccinimide (NBS) with FeCl2 as a catalyst in the latex phase (NR–Br); and an indirect method using a ring opening of epoxidized natural rubber (ENR) with 2-bromopropionic acid (ENR–Br). The chemical structure, including determination of the bromine contents, was analyzed with proton nuclear magnetic resonance and Fourier transform infrared spectroscopy. The occurrence of bromine in NR–Br was confirmed using scanning electron microscopy with energy dispersive x-ray spectroscopy. Strong emission peaks for Br Kα at 1.5 eV was evidenced. Moreover, glass transition temperature of modified NRs increased after bromination. Two types of brominated NR, that is, NR–Br and ENR–Br containing 2 and 4 mol% of bromine function, respectively, were used in a range of 1–5 phr in the silica-reinforced NR system with silica loading of 10 and 30 phr. Both cure and mechanical properties of the rubber compounds were investigated. The incorporation of the bromine function in NR of both ENR–Br and NR–Br enhanced the cure reactivity of the NR–silica vulcanization system. The modified NRs may have a role as a coupling agent between the NR and the silica filler.


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